New to Research

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Health research is about asking questions and finding new ways of improving patient care

Here at NBT, research is led by and carried out by clinical and non-clinical teams that include Nurses, Midwives, Doctors, Administrators, Clinical Trial Officers, Physiotherapists, Speech and Language Therapists, Clinical Librarians and more.

If you have an idea for research or would like to develop a career as an independent researcher, we can offer comprehensive support. This could include help with grant and training applications or navigating the research system.

We've spoken to people working in research carrying out many different roles. Read about or watch our My Role In Research colleagues.

People can become experts in their everyday surroundings, so they’re the ones best placed to solve problems or develop evidence through research. Whether you’re in a clinical or non-clinical role, we’re looking to increase the range of roles carrying out research at NBT. 

This webinar gives a good introduction to Research.

Contact research@nbt.nhs.uk for further help.

We're here to help! Here are some Frequently Asked Questions

How do I know if my study is research?

Research can be defined as the attempt to derive generalisable or transferable new knowledge to answer or refine relevant questions with scientifically sound methods. This excludes: audit; needs assessments; quality improvement and other local service evaluations. It also excludes routine banking of biological samples or data, except where this activity is integral to a self-contained research project designed to test a clear hypothesis.

If you are in any doubt, please contact the Research Development & Grants team – we can support your project or signpost you to a more appropriate team, if required. 

I am very busy in my current role, but I would like to get involved in research. Is there any way I can combine it with my day-to-day role?

Yes. There are lots of opportunities to get involved in research, including developing a project or grant application of your own, as part of your role. The R&D Department have funding available to cover your time to work in research. This would be discussed on a case-by-case basis with your department, so please get in touch with the Research Development & Grants team who can support you with conversations with your line manager and clinical division.

Do I need to have experience in research to write up a research proposal?

Research ideas and grant applications are welcome from everyone, no matter how much (or little) prior experience you have. The Research Development & Grants team can provide additional support to those that need it, especially if you are new to research.

Who should I contact to help me with costing my grant application and developing my project?

Please email the Research Development & Grants team: ResearchGrants@nbt.nhs.uk

What support can the Research Development & Grants team offer me?

The Research Development and Grants team can support you from early stages of developing a research idea. We can help to find suitable funding opportunities, calculate costs for an established proposal, and navigate systems for submitting your grant application, and much more.

When is it appropriate to reach out to the Research Development and Grants team?

Any time! From just having a brief idea for a research project, to needing final costings on a grant application. You can speak to the Research Development & Grants team at any stage of your research development. The sooner you contact us the better though, and the team will provide tailored support.

How long will it take to cost my research project for my grant application?

This is dependent on your project. But the Research Development and Grants team can support you with every aspect of your costing. The sooner you get in touch with us (i.e. as soon as you begin writing your grant application) the more support we can offer.

View Our Research

Doctor conducting research at NBT

Explore the ground-breaking research currently taking place at North Bristol NHS Trust.

About Research & Development

NBT Researcher

Find out more about our research and how we're working to improve patient care.

Contact Research

Research & Development
North Bristol NHS Trust
Level 3, Learning & Research building
Southmead Hospital
Westbury-on-Trym
Bristol, BS10 5NB

Telephone: 0117 4149330
Email: research@nbt.nhs.uk

Researcher Zone.png

Preterm Birth Prevention Clinic

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Information for before your visit 

Why have I been referred?

Our Preterm Birth Prevention Clinics offer extra care for women who may be at higher risk for preterm (premature) birth. There are several reasons why women may be at higher risk, including if you have experienced any of the following:

  • Previous preterm birth.
  • Previous prelabour, premature rupture of membranes (water breaking early).
  • Previous miscarriage after 16 weeks gestation. 
  • Previous cervical surgery including caesarean sections at full cervical dilation.
  • Uterine anomalies.
  • Shortened cervix seen on ultrasound scan.

We offer the following assessments in the clinic:

  • An internal ultrasound scan to assess the length of your cervix.
  • A urine test and vaginal swab may be taken to screen for infection.

What will happen when I visit the clinic?

Please arrive 10 minutes before your appointment time so we can take your blood pressure and perform a urinalysis. These are routine tests offered at most antenatal appointments during your pregnancy.

You will see a doctor and a specialist preterm birth prevention midwife who will discuss your risks for preterm birth, including information regarding your current and previous pregnancies. All tests offered are safe for you and your baby.

You will be offered a transvaginal ultrasound scan to measure the length of your cervix. This scan involves a small ultrasound being inserted into the vagina - it requires an empty bladder.

What treatments do you offer?

Not everyone who attends the clinic will require treatment. Depending on the initial assessment you may be offered further monitoring and reassurance with repeat ultrasound scans.

If you are at higher risk of preterm birth, you may be offered vaginal hormone (progesterone) pessaries/tablets. More rarely a stitch around the cervix may be recommended to those at highest risk of preterm birth.

When to seek advice

Sometimes there are signs that you may be going into labour. Often the signs may not lead to preterm birth, but it’s important to seek urgent advice. These signs may include:

  • Period-like pains or cramps which come and go.
  • Constant back pain.
  • Fluid leaking from the vagina.
  • Bleeding from the vagina. 

If you think you may be in labour, do not wait for your next appointment. You should call the Central Delivery Suite at Southmead Hospital on the same day. The phone number is on the front of your yellow maternity notes. 

Should I still attend my antenatal appointments?

Yes, you should.

Lifestyle modifications

Many of the risks for preterm birth cannot be changed, however there are some lifestyle changes that can be made where possible.

  • Smoking has been associated with preterm birth, and therefore cutting down or stopping smoking is a positive step that can be taken to reduce the risk of your baby being born prematurely. You can speak with your midwife or with the doctor at the preterm birth prevention clinic for advice and ask for a referral for support with giving up smoking. 
  • Drinking alcohol during pregnancy has been associated with premature birth. Drinking no alcohol at all is safest. 
  • Tooth decay and gum disease has been associated with preterm birth, and therefore it is a good idea to see your dentist, especially if you think you may have tooth decay or toothache. You can organise free dental care with your maternity exemption card.

© North Bristol NHS Trust.  This edition published December 2024. Review due December 2027. NBT003698.

Contact Preterm Birth Prevention Clinic

Preterm Birth Prevention Clinic
Foetal Meicine Unit
Cotswold Outpatients,
Southmead Hospital
Westbury-on-trym
Bristol
BS10 5NB

0117 414 6928

Contact Severn Pathology

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Use of email

Our NBT email address has been accredited to the NHS Digital Accreditation Standard DCB1586 (The secure email standard - NHS Digital) so you can be assured when sending confidential information to us that this is as secure as NHS.net.

See individual department pages for telephone numbers and appropriate emails.

 

Address and location

Severn Pathology
Pathology Sciences Building
Southmead Hospital
Westbury-on-Trym
Bristol
BS10 5NB

Pathology Opening Hours

See specific departmental information for detailed contact information and availability.

A summary of opening hours are as follows:

For Blood Sciences departments (Chemistry, Haematology, Blood Transfusion and Specimen Reception) please see the following:

 

Microbiology: 8am–8pm weekdays out of these hours and Bank Holidays contact via NBT Switchboard.

Cellular Pathology: 9am-5pm out of these hours and Bank Holidays contact via NBT Switchboard.

Switchboard: 0117 9505050

Test Information

Community Acquired Pneumonia Research Priority Setting Project

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We are looking for people who have lived experience of Community Acquired Pneumonia. 

We would like you to join a group of health professionals to help us to see what research would make a difference to adults who have lived experience of community acquired pneumonia.

What is community acquired pneumonia? 

Community acquired pneumonia is the commonest reason that people are admitted to hospital in the UK. It is an infection of one or both lungs that is usually caused by bacteria and viruses. We call it community acquired because people who get it are living in the community as opposed to being in hospital at the time. 

What are we asking you to do? 

We are anticipating that the group will meet monthly for approximately 12 – 18 months. Most of the meetings will be held on-line (virtually) and will take no more than two hours per meeting. 

There may occasionally be face to face meetings which will be a little longer, to make good use of the opportunity to work together in this way. Travel expenses will be reimbursed, and you will also be compensated for your time with non-cash transferable vouchers as a way of saying thank you for your time. 

What do you need to do now? 

Who is funding the project? 

James Lind Alliance and Southmead Hospital Charity 

The James Lind Alliance is non-profit making initiative bringing patients, their families and carers, and clinicians together in a Priority Setting Partnership (PSP) to identify and prioritise uncertainties, or ‘unanswered questions’, about Community Acquired Pneumonia  that have not been answered by previous research, and are important to patients, their families and carers with lived experience, and professionals who look after them. 

Southmead Hospital Charity 

The Charity will be working closely with the Health Professionals and the James Lind Alliance to list  all the possible areas for research will then be discussed and the top 10 prioritised. This will ensure that researchers and those who fund research, focus on what really matters to both patients and clinicians. 

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About The Pain Clinic

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This information is for patients who have been referred to the Pain Clinic.

Pain Clinic Services 

Your appointment

Pain that persists can be distressing and disabling. You have been referred to the pain service because your pain is interfering with your ability to function effectively. We are a team of specially trained healthcare professionals who are skilled in supporting patients with pain to manage their symptoms. Most of the treatments we offer will help about one third of patients only and will reduce the intensity of pain but not take it away. Response to treatment varies from person to person, even if they seem to have the same symptoms. Your pain specialist will make an assessment of you and of your pain and decide which treatment or treatments might be helpful in your case. 

Injections may help some individuals but they often only have a limited effect and should be part of a multidisciplinary management programme. A decision on an injection will only be made after a full discussion with the patient if it is considered appropriate.

With support, patients can start to exercise, engage with hobbies and resume work (full or part-time). Our aim in this service is to help people move forward and for this reason it is unhelpful for us to disable our patients by saying they are unfit to work.

Our service works to support you and your GP to manage your pain. The treatments we offer are familiar to your GP and your GP will be experienced in managing day-to-day queries about your pain treatment. Your pain specialist may make a pain treatment plan for you and your GP to follow together. Your GP will be able to deal with queries and if you have a problem with medication you can also discuss this with 
your pharmacist.

Service objectives

  • Provide a multi-professional patient specific assessment of your pain and out in place an individual management plan. 
  • We help you to manage your pain enabling you to lead a more normal life with reduced disability. 
  • Increase social and physical functioning. 
  • Promote independence and wellbeing for patients through the provision of structured self-management support. 

In our team we have the following staff: 

  • Consultants in pain medicine.
  • Consultants in neurosurgery.
  • Specialist physiotherapists.
  • Specialist Pain Nurses.
  • Clinical psychologists.
  • Pharmacists.

You will not necessarily see more than one specialist, but as one of the major pain centres in the UK, we are able to adopt a multidisciplinary approach for those patients who need it. 

Can you keep your appointment?

If you cannot attend your appointment please phone and tell us as soon as you can. We can rearrange your appointment and offer your old appointment to another patients. 

Phone: 0117 414 9937

If you do not attend your appointment or cancel on the day of the appointment, we will have to discharge you back to your GP. You will then have to ask to be referred again.

Please let us know if you change your:

  • Name.
  • Address.
  • Phone number.
  • GP. 

Preparing for your appointment

Please think about the following things and write them down to bring to your appointment: 

  • Have you attended a Pain Clinic before? If you have please write down the name of the Pain Clinic, the year you attended, and the name of the doctor you saw.
  • A list of all the medicines (if any) you take, even they are not for pain. 
  • A list of all the medicines you have tried for pain.
  • A list of all the other treatments you have tried for pain e.g. acupuncture, TENS, physiotherapy.
  • You could use a diagram to mark where in your body you feel pain.
  • Have you had to change, reduce, or stop any of your activities (including exercise, socialising, housework, leisure etc.)? 
  • As a consequence of living with pain, people often experience feelings of anger, frustration, anxiety and/or low morale. How would you say you were at the moment in terms of emotions or mood?

Further management

Management of your pain will be discussed at your appointment. You will be given a blue form to take to the reception desk to make an appointment for further treatment if this is appropriate. If you are referred to the Pain Management team an appointment for an assessment will be sent to you in the post.

Comments

We want to know what we are doing well and what we ought to be improving. Please help us to provide a service that matches what our patients need. There is a comments box in the waiting area. You can also speak to a member of staff if you wish to make a comment about the service you have received. 

© North Bristol NHS Trust. This edition published February 2024. Review due February 2027. NBT002044

 

Contact Pain Clinic

For all appointment enquiries, please contact Outpatients appointments.

Gloucester House
Southmead Hospital
Telephone: 0117 4147361

If you have an urgent concern please seek medical advice from your GP.

Uterine Fibroid Embolisation (UFE)

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Information for patients about Uterine Fibroid Embolisation (UFE). 

What are fibroids?

Fibroids are benign, non cancerous, fibrous growths of the muscular part of the uterus (womb). They are very common.

How are fibroids diagnosed?

The diagnosis is made with an ultrasound scan or an MRI scan. Other tests such as blood tests, a gynaecological examination  or internal biopsy may also be necessary.

Why do fibroids need to be treated?

Many fibroids do not cause any symptoms at all, and don’t require treatment as they are benign. Often fibroids are found by chance as part of an examination for other reasons, e.g. pregnancy scanning.

The most common symptom is heavy and prolonged periods, which may be more painful than usual. This can cause anaemia (a lack of red blood cells or the chemical haemoglobin, which is found in the blood). It can make you feel tired and faint or cause headaches.

Large fibroids can cause symptoms because of their size putting pressure on the bladder leading to a constant urge to urinate. They may also push on your spine or back passage causing constipation and bloating. Occasionally, fibroids may be so large that they are visible as a swelling in the abdomen.

Fibroids are also associated with infertility and miscarriage.

How are fibroids treated?

If the gynaecologist does advise treatment, options include:

  • Drug treatment: A variety of hormonal drugs can be used to manage the symptoms of fibroids and sometimes even allow them to shrink. Often these medications can be started and monitored by your GP. The decision about whether this is right for you will depend on your specific symptoms and personal preferences for treatment
  • Intrauterine contraceptive device: A Mirena coil releases progestogens and may help to reduce heavy bleeding. The coil can be left in place if you are to proceed to UFE.
  • Myomectomy: In some cases it may be possible to surgically remove fibroids (myomectomy) without taking the uterus itself. This means that future pregnancyremains possible. However, it is important to understand that hysterectomy (removal of the uterus) may very occasionally be necessary at the time of myomectomy.
  • Fibroids may regrow after myomectomy, and in the long term about 1 in 10 people require further surgery. Myomectomy may be performed as an open operation, or by a keyhole technique. This procedure is particularly successful if there are one or two symptomatic fibroids, but is less successful if there are multiple fibroids.
  • Hysterectomy: This is the surgical removal of the uterus, usually including the cervix. Future pregnancy is impossible. The operation usually requires about 2-3 days in hospital and 4-6 weeks off work afterwards Uterine Fibroid Embolisation (UFE): as discussed next.

What is Uterine Fibroid Embolisation (UFE)?

Fibroid embolisation is a procedure designed to shrink uterine fibroids and reduce bleeding. A small plastic tube is placed into a blood vessel (artery) in the groin or the wrist and used to access the blood supply to the uterus and the fibroids. This blood supply is then blocked with extremely tiny beads made of polyvinyl alcohol (PVA) and will permanently stay in the small arteries within the fibroids.

 

What are the benefits?

  • There are now good long-term studies of the results of fibroid embolisation. Over 80% of people will be relieved of their symptoms after UFE.
  • On average, UFE shrinks the fibroids by about half and this usually gives an improvement in symptoms relating to the size of the fibroids or pressure.
  • Unlike other surgical treatments for fibroids, UFE treats all the fibroids in a person’s uterus.
  • Successful pregnancy can be possible after fibroid embolisation.

What happens before the procedure?

You will need to have a blood test a few days before the procedure to check your kidney function and your haemoglobin levels. This may be arranged to take place at your GP surgery.

You can continue taking your normal medication. If you are on any medication which thins the blood (e.g. aspirin, clopidogrel, warfarin, rivaroxaban, dabigatran, apixaban) we ask you to call the Imaging Department using the number on your appointment letter as we may need to adjust your medication before undergoing this procedure.

On the day of the procedure

  • You should not eat anything from 6 hours before your procedure but you may continue to drink water up to 2 hours beforehand.
  • You will arrive at the Imaging Department (Gate 19) and be accompanied into our day case area.
  • You may take your normal medication unless instructed otherwise.
  • Please inform us if you have any allergies.
  • A radiologist (X-ray doctor) will discuss the procedure with you. You will have an opportunity to ask questions about the procedure and your treatment. If you choose to have the procedure you will need to sign a consent form (this may already have been filled out in an earlier clinic consultation).
  • You will be asked to change into a hospital gown and a small plastic tube (cannula) will be put into a vein in your arm to allow us to administer medications or intravenous fluids during the procedure.
  • A drip containing strong pain killers (patient controlled analgesia - PCA) will be connected to your cannula, which will allow you to manage your own pain after the procedure by pushing a button that injects a small dose of morphine into your vein. We will give you an extra pain killer via a pessary (diclofenac) as well.
  • Once all the checks have been performed and consent signed, you will be taken to the procedure room on the trolley. There will be nurses, a radiographer and the radiologist with you throughout the procedure.

During the procedure

  • You will be asked to lie on your back on an X-ray table for the duration of the procedure.]
  • The skin near the groin/wrist will be cleaned with an antiseptic solution and covered with sterile drapes.
  • Using an ultrasound machine, the radiologist will then inject local anaesthetic into the skin and deeper tissues over the groin/wrist artery. This will briefly sting and then go numb. Most people will feel a pushing sensation.
  • A small tube (catheter) is inserted into the artery and navigated inside your blood vessels with the help of the X-ray machine to select the arteries responsible for the blood supply of the fibroid(s).
  • An X-ray dye will be injected into your arteries several times during the procedure to help outline your anatomy.
  • During these injections you may be asked to hold your breath and keep very still. The injection of the X-ray dye can cause a hot sensation in your pelvic area which is normal and temporary.
  • Once the catheter is in the correct position, tiny PVA beads are slowly injected to block the arteries supplying the fibroid(s).
  • It might be necessary to access the arteries in both groins in order to block the arteries on both sides of the uterus which are supplying the fibroid(s).
  • When the procedure is complete, the catheter is removed from the artery and pressure by hand or a special stitch is applied at the puncture site to prevent bleeding.
  • The procedure itself usually takes around 1-2 hours.

What to expect after the procedure

  • You will be taken back to the day case area, so that nursing staff may monitor you closely.
  • You will be required to lie flat for 2 hours to allow the small hole in your artery to heal but you can mobilise 4 hours after the procedure.
  • You may experience pain similar to period cramping in your lower abdomen, but this can be controlled with your PCA morphine pump. Additional pain killers can be given if required.
  • Later on you will be transferred to the gynaecology ward (Cotswold ward) where you will stay at least 1 night so we can ensure adequate pain relief is available to you.
  • Most patients are normally discharged just after lunch the following day.
  • There may be a small bruise in the groin/wrist around the puncture site but this is quite normal.

Will I feel any pain?

You will be given strong painkillers before, during and after the procedure designed to minimise any pain. If you are in pain at any point this medication can be adjusted to ensure your pain is controlled. The local anaesthetic used to numb groin/wrist may sting for about 20 seconds.

What to expect in the days following UFE

Mild pain or discomfort is usual for some days after the procedure, which can be managed with standard pain killers like paracetamol and ibuprofen.

Some patients experience a thick yellow/green vaginal discharge. Use sanitary towels rather than tampons as these could increase the risk of infection.

You may have a slightly raised temperature for up to a week afterwards, sometimes with feverish symptoms.

You may feel tired and we advise you to rest for one to two weeks depending on your recovery. You can then resume your usual activities. We usually recommend taking up to 2 weeks off work but some people recover more quickly and are able to return to work within a week.

You will be followed up via in person or telephone clinic by the radiologist in 4-6 months after the procedure.

When will I notice a difference?

It takes time for fibroids to shrink after UFE. It is common for the first period after UFE to be a little different from usual.

Gradual improvement can be expected for up to 6 months afterwards.

What are the risks?

UFE is generally very safe however as with any procedure there are some risks.

  • There is a minor risk of bleeding or bruising at the groin/ wrist or injury to the arteries.
  • Most patients feel some pain afterwards. This ranges from very mild pain to severe cramp, period-like pain. This pain is usually most severe during the first 12 hours, and will be controlled with strong painkillers. By time of discharge home the following day, ‘over the counter’ painkillers are usually adequate to control the pain.
  • Infection is a risk with any operation. Currently there is a quoted risk of about 2%. Antibiotics are given at the time of the UFE to minimise this risk but late infection some weeks afterwards has been reported. Most infections can be treated with antibiotics at the time but rarely patients will need to have a hysterectomy for infection. If you feel you would not like to have a hysterectomy under any circumstances then it is probably best not to have a fibroid embolisation.
  • You may experience post-embolisation syndrome. This is caused by the breakdown of the fibroid within the body and is very common. People experience a mild fever and flu-like symptoms. It usually passes on its own and anti-inflammatory medicines (ibuprofen) can help. If your symptoms continue, please contact us so we can make sure you don’t have an infection.
  • There is a small risk of blocking blood vessels to other organs inside your pelvis (including urinary bladder, bowel or genitals). This could result in reduced blood supply to the affected organ and could potentially be a serious complication, however in most cases it settles down by itself. A special CT scan of your blood vessels will be used during the procedure to reduce this risk to a minimum.
  • Rarely a patient may have an allergic reaction to the X-ray contrast (dye) used during UFE. This reaction could be mild with itching to severe affecting breathing or blood pressure. Patients undergoing UFE are carefully monitored throughout the procedure so any allergic reaction can be detected immediately and treated.
  • About 1% of patients have an early menopause as a result of UFE. This risk is smaller in younger people and higher in patients who are approaching the menopause. 
  • Rarely patients may pass bits of fibroid after the UFE. If a larger fibroid is passed you may need to see your gynaecologist who can help to remove it.
  • Some patients experience vaginal discharge, which usually lasts up to 2 weeks and on occasion up to 4 weeks.

Can I have UFE if I want to get pregnant?

It is possible to have a successful pregnancy after fibroid embolisation. Current advice is to wait at least 1 year after the procedure before trying to conceive. Approximately 50% of people trying to conceive after fibroid embolisation will be successful.

There is evidence that the rate of spontaneous abortion or miscarriage is higher among patients having fibroid embolisation than in patients who have a surgical myomectomy. If you want to conceive then depending on the anatomy of your uterus and fibroids, myomectomy may be a better procedure.

Further information for patients after uterine fibroid embolisation (UFE)

You may find the following information useful after going home from hospital after a UFE.

Eating and drinking

You should not eat or drink until the conscious sedation medication has entirely worn off. The antibiotics may make you feel nauseated, so it is best to avoid alcohol for 24 hours.

Driving

You should not drive or operate machinery for at least 2 days after this procedure; this means you should ask for a relative or friend to drive you home from hospital. It is important you ensure you can perform an emergency stop prior to any driving.

Your groin

If we do the procedure through the artery in your groin,  You may have bruising or swelling in the first few days at the puncture site. If you are worried about this call the ward.

Vaginal discharge

It is common for patients to experience a moderate vaginal discharge after this procedure, which may be blood stained or contain small pieces of fibroid. If the discharge becomes more offensive and smelly it is important that you contact the ward as this may indicate you are developing an infection.

Pain

The purpose of staying overnight in hospital after UFE is to ensure you are pain free. Make sure you have paracetamol and ibuprofen at home. The ward will give you further painkillers to take home with you should you need them. Should the pain worsen following discharge home call the ward for further advice.

Fever

It is common to experience a low grade temperature for up to 1 week after this procedure. You may have flu like symptoms. If you have a high temperature (above 37.5°C) more than 7 days after the procedure it may indicate that you are developing an infection so you should contact the hospital.

Sexual intercourse and contraception

You can resume sexual activity when you feel ready and once the discharge has settled.

It is important to use appropriate contraception for one year after UFE.

If you do not want to get pregnant you will still need to use contraception.

Please check with your travel insurance if you wish to travel within 4 weeks of your procedure

Finally we hope this information is helpful.

If you have any questions either before or after the procedure the staff in the Imaging department will be happy to answer them.

The phone number for the Imaging department can be found on your appointment letter.
 

© North Bristol NHS Trust.  This edition published February 2024. Review due February 2027. NBT002898.
 

Contact Cotswold Ward

Cotswold Ward
Brunel building
Southmead Hospital
Westbury-on-trym
Bristol
BS10 5NB

0117 414 6798 (24 hours) 

Prostate Artery Embolisation (PAE)

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This information is for patients considering Prostate Artery Embolisation (PAE) for the treatment of their lower urinary tract symptoms.

What is Prostate Artery Embolisation (PAE)? 

The prostate gland is located under the urinary bladder and wraps around the water pipe (urethra). Enlargement of the prostate gland can lead to a blockage of the flow of urine. This can lead to various symptoms, including reduced urine stream and frequent need to urinate during the night.

Prostate artery embolisation is a minimally invasive, non-surgical new treatment option for prostate enlargement. PAE blocks off the blood flow to the small arteries supplying the prostate gland making the gland shrink and allowing a better flow of urine.

This is achieved with an injection of small particles into these arteries. PAE can also be used for controlling bleeding from the prostate gland.

Who made this decision?

The decision was made by your urologist and an interventional radiologist who is going to perform the procedure.

Interventional radiologists are doctors specially trained to perform minimally invasive treatments of various diseases with guidance of an x-ray machine, avoiding the need for open surgery. This includes inserting and navigating special catheters inside blood vessels.

In addition to the standard tests for prostate enlargement, you will need to have a special CT scan (CT angiogram) to help us visualise the arteries in your pelvis. This will help the radiologist to decide if the anatomy of your arteries is suitable for the treatment. If tests have shown that you are suffering from an enlarged prostate gland you probably have already been told about the more traditional treatment options, including a

TURP (trans urethral resection of prostate) operation and medication by your urologist or GP.

In your case, a decision was made that you are likely to benefit from an alternative non-surgical treatment option: prostate artery embolisation.

What happens before the procedure?

  • You will need to have a blood test a few days before the procedure to check your kidney function, that you are not at increased risk of bleeding and that it will be safe to proceed. This may be arranged to take place at your GP surgery.
  • You can continue taking your normal medication. If you are on any medication which thins the blood (e.g. aspirin, clopidogrel, warfarin, rivaroxaban, dabigatran, apixaban) we ask you to call the imaging department using the number on your appointment letter as we may need to adjust your medication before undergoing this procedure.

On the day of the procedure

  • You should not eat anything from 4 hours before the procedure but you may continue to drink water.
  • You will arrive at the Imaging Department and be accompanied into our day case area.
  • You may take your normal medication unless instructed otherwise.
  • Please inform us if you have any allergies.
  • A radiologist will discuss the procedure with you. You will have an opportunity to ask questions about the procedure and your treatment. If you choose to have the procedure you will need to sign a consent form.
  • You will be asked to change into a hospital gown and a small plastic tube (cannula) may be put into a vein in your arm to allow us to administer medications or intravenous fluids during the procedure.
  • Once all the checks have been performed and consent signed, you will be taken to the angiography suite on the trolley. There will be a nurse, radiographer and a radiologist with you throughout the procedure.

During the procedure

  • You will need to lie on your back on an X-ray table for the duration of the procedure.]
  • The skin near the groin will be cleaned with an antiseptic solution and covered with sterile drapes.
  • Using an ultrasound machine, the radiologist will then inject local anaesthetic into the skin and deeper tissues over the groin artery. This will briefly sting and then go numb. Most people will feel a pushing sensation.
  • A small tube (catheter) is inserted into the artery and navigated inside your blood vessels with the help of the x-ray machine to select the arteries responsible for the blood supply of the prostate gland. An x-ray dye will be injected into your arteries several times during the procedure to aid the navigation of the catheter. During these injections you may be asked to hold your breath and keep very still. The injection of the x-ray dye can cause a hot sensation in your pelvic area which is normal and temporary.
  • Both the left and right prostate arteries can usually be reached with accessing only one groin artery but sometimes we may need to use the artery in your other groin.
  • Once the catheter is in the correct position, tiny particles are slowly injected into the prostate gland. When the injection into both left and right prostate arteries is complete, the catheter is removed from the artery and pressure by hand or a special stitch is applied at the puncture site to prevent bleeding. You will be asked to remain still for another few hours after the procedure.
  • Insertion of a urinary catheter may be necessary for this procedure. This is usually removed after the procedure before discharge.

What to expect after the procedure

  • You will be taken back to the radiology day case unit, so that nursing staff may monitor you closely.
  • If you are in pain tell the nursing staff so you can be given appropriate painkillers.
  • You will be required to stay in our day case unit for about 4 hours. Occasionally one night stay in the hospital might become necessary.
  • There may be a small bruise in the groin around the puncture site but this is quite normal.
  • You will have antibiotics prescribed to be taken for 5-7 days following the procedure.
  • You should be able to resume most normal daily activities within 24-48 hours. However, we recommend avoiding driving and all strenuous activities for 48 hours.
  • The prostate gland should begin to shrink over the next few weeks and over 70% of men will notice an improvement in their symptoms after PAE.
  • You will be reviewed at a follow up appointment in 3 months’ time.
  • If you had a long-term bladder catheter before the procedure, recent studies have shown the majority of patients can have their catheters removed after 7-10 days.
  • Please check your travel insurance if you wish to travel within 4 weeks of your procedure.

Prostate artery embolisation is a relatively new procedure for treatment of prostate enlargement. The current evidence from research data has been reviewed by the National Institute for Health and Care Excellence (NICE) and clearly shows that the procedure is safe and an effective treatment option. 

However, as with any other medical procedures complications may arise:

  • There is a minor risk of bleeding or bruising at the groin or injury to the arteries.
  • In up to 10% of cases (1 in 10 people) the prostate arteries are too small or diseased and it will not be possible to safely access them with the catheter, meaning we are unable to treat the arteries.
  • You may experience some discomfort in the lower abdomen and have some discomfort on urinating but this normally resolves after 10 days.
  • The prostate can become more swollen immediately after the procedure which can make passing urine temporarily more difficult. On rare occasions, a urinary catheter may be necessary until the swelling settles down.
  • There is a small possibility of experiencing pain when passing urine or having blood in the urine after the procedure but this should settle down by itself.
  • Blocking arterial flow to the prostate makes the gland slightly more prone to infection. To avoid this, antibiotics will be prescribed for you to take when you arrive at the department and following the procedure.
  • There is a small risk of blocking blood vessels to other organs inside your pelvis (including urinary bladder, bowel or genitals). This could result in reduced blood supply to the affected organ and could potentially be a serious complication, however in most cases it settles down by itself. A special CT scan of your blood vessels will be used before and during the procedure to reduce this risk to a minimum.
  • Some patients may feel tired for up to a week following the procedure. We advise patients to take at least one week off work following PAE.

When to seek help

Please contact us on the phone number on your appointment letter if you experience: 

  • New bleeding in your urine or bowel motions.
  • Pain that is not controlled with painkillers.

Please contact us or go to the nearest emergency department in case of:

  • New leg symptoms such as pain or changes in colour.
  • Increasing swelling or bleeding from your groin.

To contact us, please call the interventional radiology secretaries between:

Monday-Friday 9am-5pm on 0117 414 9110.

Out of hours please contact the on call urology specialty registrar via North Bristol NHS Trust switchboard on 0117 950 5050.

 

References

  1. NICE (2018) “Interventional procedure overview of prostate artery embolisation for lower urinary tract symptoms caused by benign prostatic hyperplasia” https://www.nice.org.uk/guidance/ ipg611/evidence
  2. Ray et al (2018) “Efficacy and safety of prostate artery embolization for benign prostatic hyperplasia: an observational study and propensity-matched comparison with transurethral resection of the prostate (the UK-ROPE Study)” BJU Int 2018; 122: 270-282
     

© North Bristol NHS Trust.  This edition published January 2024. Review due January 2027. NBT003172.

Paclitaxel-coated balloons or stents

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This page is for patients whose vascular surgeon or interventional radiologist thinks they would benefit from treating a narrowing in their blood vessel with special balloon or stent coated with a drug called paclitaxel. We hope to following information will answer some of the questions you may have about this procedure.

What is paclitaxel? 

Paclitaxel is a drug used to prevent the smooth muscle cells in your blood vessel from growing. If these cells were to grow, it could cause another blockage in your blood vessel.

Research studies show that balloons and stents coated with paclitaxel increase the chance that the treated blood vessel will remain open after your treatment. This could lower the likelihood that you will need a repeat procedure to re-open the vessel in the future.

Are there any risks or complications associated with paclitaxel-coated balloons or stents?

The risks of having an angioplasty or a stent insertion are outlined in the angiography and angioplasty patient information leaflet which you have also received. There are potentially additional risks with having a paclitaxel-coated balloon or stent.

Based on the result of a single study published in 2018¹ there is a possibility that the use of balloons and stents coated with paclitaxel may increase your chance of death about 2 years after treatment.

When compared to treatment with uncoated balloons or bare metal stents there is also information that suggests that the use of these balloons and stents coated with paclitaxel may increase your chance of death over the next 2-5 years.²

This study¹ has several limitations, its results are widely debated, and further research is still ongoing.

Your doctors believe that the benefit of using a balloon or stent coated with paclitaxel would outweigh the potential increased risk of death shown in the previously mentioned research paper. This is by improving the likelihood that your vessel remains open after the treatment for longer, either because:

  • Other treatment options without paclitaxel have already been tried and failed.
  • Other treatment options, including bypass surgery, would not be technically possible or would be even riskier for you.
  • Not treating the narrowing in your blood vessel would likely cause you significant permanent damage or a condition that would threaten your limb or even your life.

Are there any other options?

There may be other options for the treatment of your symptoms including medications, exercise, balloons, stents or other devices that do not contain paclitaxel and surgery. You should discuss with your doctor the possible risks and benefits of all treatments to identify those options that are best for you.

References

(1) Katsanos K, Spiliopoulos S, Kitrou P, Krokidis M, Karnabatidis D. Risk of death following application of paclitaxel-coated balloons and stents in the femoropopliteal artery of the leg: a systematic review and meta-analysis of randomized controlled trials. J Am Heart Assoc 2018;7(24):e011245-e011245. 

(2) MHRA statement : Paclitaxel drug-coated balloons (DCBs) or drug-eluting stents (DESs): Reconfirmed position on use in patients with intermittent claudication and critical limb ischaemia (DSI/2021/001) Paclitaxel drug-coated balloons (DCBs) or drug-eluting stents (DESs): Reconfirmed position on use in patients with intermittent claudication and critical limb ischaemia (DSI/2021/001) - GOV.UK (www.gov.uk)

© North Bristol NHS Trust. This edition published June 2022. Review due June 2025. NBT003453.

Nasogastric/nasojejunal tube insertion

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This information is for patients whose doctor has requested you have a nasogastric/nasojejunal tube inserted.

What is a nasogastric/ nasojejunal tube?

A nasogastric (NG) tube is a narrow feeding tube which is placed through your nose down into your stomach. 

A nasojejunal (NJ) tube is also a narrow feeding tube placed through the nose, but it is positioned in the small bowel beyond stomach (the jejunum).  

These feeding tubes can be used to give you fluids, medications and liquid food complete with nutrients directly into your stomach or small bowel, as appropriate.

Why do I need to have an NG/ NJ feeding tube inserted?

NG/ NJ tubes can provide you with the fluids, medications and nutrition your body needs while you are unable to eat or drink adequate amounts. 

This may be because you have swallowing problems or need access for specific medications such as Duodopa, or need additional nutritional support.  

Are there any risks?

NG/ NJ tube insertion is a safe procedure.

On the day of the procedure

Please inform us if you are allergic to anything or you are diabetic.

  • You should not eat for 4 hours before your appointment. 
  • You may drink water and take any prescribed medications until the time of your appointment. 
  • If you are an outpatient, you will arrive at the Imaging Department, Gate 19 of the Brunel building and be accompanied into our day case area. 
  • If you are an inpatient, you will come to the Imaging Department from the ward you have been admitted to.
  • A doctor will discuss the procedure with you. You will be given an opportunity to ask any questions you may have. 
  • Once all the checks have been performed, you will be taken to the procedure room. 
  • There will be a doctor, nurse and radiographer with you throughout the procedure.
  • You will be given a local anaesthetic throat spray to help numb the throat.
  • Some lubricant jelly will be put on the tube to help it into position.
  • The narrow feeding tube will be passed through a nostril, down into your stomach/ small bowel guided by an x-ray machine. You will be asked to swallow a few times to help the tube into position. 
  • The tube will then be secured using a dressing or nasal tape.

What happens after the procedure?

You will be taken back to the day case area or your ward, so that nursing staff may monitor you closely.

We hope this information is helpful. If you have any questions before or after the procedure, please phone the Imaging Department using the number on your appointment letter.

© North Bristol NHS Trust.  This edition published December 2022. Review due December 2025. NBT003519

Medial branch blocks (Imaging)

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What is a medial branch block? 

This procedure is for diagnosis only and is not for permanent pain relief. Your pain is likely to return a few hours after the procedure.

Facet joints are found between each of the spinal bones and allow the spine to move. The medial branches are nerves that carry information, including pain, from the facet joints to the brain. Sometimes back pain arises from these joints. 

A medial branch block uses local anaesthetic to numb these small nerves. 

If the pain is coming from the joints the pain may be reduced for some hours following these injections.

Following this procedure we can determine whether the facet joints are the cause of your pain.

Depending on the results, your consultant may offer a longer-lasting treatment that could be done after your follow up call or visit.

How do I prepare for the medial branch blocks?

We would advise you not to take any pain relief medication for 6 hours before your appointment.  This is so we can accurately assess if the local anaesthetic changes your back pain. You can eat and drink on the day as normal. You are advised not to drive following the procedure.

Please tell us before attending for the procedure if you take any blood thinning medication such as:

  • Warfarin.
  • Clopidogrel.
  • Rivaroxaban.
  • Dipyridamole.
  • Dabigatran.


Please note this list is not exhaustive. 

The number for the Imaging department is on your appointment letter.

What will happen during the procedure?

  • You will arrive at Gate 18 where a member of the Imaging team will take you through to the fluoroscopy waiting room.
  • Following confirmation of your details and history you will be shown into the X-ray room and introduced to the staff performing the procedure.
  • You will be cared for by a small team including a radiologist (X-ray doctor) and/or radiographer and an imaging support worker.
  • Before the examination begins the radiologist or specialist radiographer will explain what they are going to do. You will be given the opportunity to ask any questions you may have. If you are happy to proceed you will be asked to sign a consent form. We will also ask you to score you back pain out of 10 before we begin. 
  • You will then be asked to lie on your front on the X-ray couch. The skin will be cleaned and a small amount of local anaesthetic will be injected under the skin. This stings for a few seconds and the area then goes numb.
  • A very fine needle will be directed to the medial branches using the X-ray machine.
  • When the radiologist or specialist radiographer is satisfied with the needle position, the local anaesthetic will be injected. Following the procedure we will ask you again to score your pain out of 10. 
  • Afterwards you will be asked to sit in our waiting room for 20 - 30 minutes so that we can ensure you are feeling well before you go home.

Will it hurt?

You may have some discomfort during the procedure. If you feel uncomfortable, let one of the members of the team know and they will try to make you more comfortable.

How long will it take?

You will be awake throughout the procedure, which lasts about 15 – 30 minutes.

How will I feel after the injections? 

Remember that medial branch blocks are not a treatment.  They are done to help us diagnose the source of your pain.
Immediately after the injections you may feel less pain but it will probably return after a few hours.

Are there any risks or side effects?

Generally it is a very safe procedure, but as with any treatment there are risks or side effects:

  • An increase in your pain in the first 24 hours following injection. Should this occur, take your usual or prescribed pain medication and seek advice from your pharmacist or GP if necessary.  
  • Bleeding or haematoma (a bruise under the skin) – this should settle down by itself.
  • Infection developing at the injection site. This will happen to less than 1 in 5000 people. Contact your GP if you experience any redness or tenderness at the injection site.  
  • The procedure is performed under X-ray to confirm the needle is in the correct place. Patients who are or may be pregnant should inform the department before attending their appointment.

Who should I contact if I have any concerns?

If you have any concerns please contact the Imaging Department using the number on your appointment letter.

© North Bristol NHS Trust.  This edition published February 2024. Review due February 2027. NBT003581.